Identification of a Novel GJA8 (Cx50) Point Mutation Causes Human Dominant Congenital Cataracts

Por Ge, Xiang-Lian, Zhang, Yilan, Wu, Yaming, LV, Jineng, Zhang, Wei, Jin, Zi-Bing, Qu, Jia, Gu, Feng
Publicado em 2014

AAV-Mediated Lysophosphatidylcholine Acyltransferase 1 (Lpcat1) Gene Replacement Therapy Rescues Retinal Degeneration in rd11 Mice

Por Dai, Xufeng, Han, Juanjuan, Qi, Yan, Zhang, Hua, Xiang, Lue, Lv, Jineng, Li, Jie, Deng, Wen-Tao, Chang, Bo, Hauswirth, William W., Pang, Ji-jing
Publicado em 2014